NDC product
Hydralazine Hydrochloride
NDC 0182-0555 · Goldline Laboratories, Inc.
Key facts
| Product NDC | 0182-0555 |
|---|---|
| Proprietary name | Hydralazine Hydrochloride |
| Labeler | Goldline Laboratories, Inc. |
| Marketing category | ANDA |
| Application number | ANDA088468 |
| Marketing start | May 1, 1984 |
| Marketing end | Feb 19, 2014 |
| Listing certified through | Feb 19, 2014 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: